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Pharmaceutical Care Program for Type 2 Diabetes Mellitus

Evaluation of Pharmaceutical Care Program for Type 2 Diabetes Mellitus in Dhule

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02435693
Acronym
pcp
Enrollment
600
Registered
2015-05-06
Start date
2012-07-31
Completion date
2015-11-30
Last updated
2015-11-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

DIABETES MELLITUS, TYPE 2

Keywords

pharmaceutical care

Brief summary

Evaluation of Pharmaceutical Care Program for Type 2 diabetes mellitus in Dhule Objectives:- 1. To evaluate Pharmaceutical care program in Type2 diabetics. 2. To evaluate the impacts of Pharmaceutical care on quality of life (QOL) in patient with Type-2 Diabetes Mellitus. 3. To study the prevalence of Type2 diabetics cases in Dhule. 4. To study the Assessment of different type of adverse drug reactions (ADRs). In Type2 diabetics. 5. To evaluate the Drug Drug intereaction in Type-2 Diabetes Mellitus. 6. To study the impacts of Pharmaceutical care program on glycemic control in patients with Type-2 Diabetes Mellitus. 7. To study the Drug utilization pattern in Type-2 Diabetes Mellitus in civil hospital Dhule. 8. To compare the efficiency of Pharmaceutical care program and drug in patients with Type-2 Diabetes Mellitus. 9. To study the Pharmaco-economic evaluation in Type-2 Diabetes Mellitus patient's. 10. To increase the patient compliance and positive attitude of patients towards the diabetes disease by counseling.

Detailed description

To evaluate the impacts of Pharmaceutical care on quality of life (QOL) in patient with Type-2 Diabetes Mellitus. To study the prevalence of Type2 diabetics cases in Dhule. To study the Assessment of different type of adverse drug reactions (ADRs). In Type2 diabetics. To evaluate the Drug Drug intereaction in Type-2 Diabetes Mellitus.

Interventions

OTHERPHARMACEUTICAL CARE programe

The pharmaceutical care program was characterized by face to face monthly visits to collect information, register information, prepare plan of care for every health problem; identification of drug therapy problems, communication to prescribers the drug therapy problems identified and education of participants to resolve the drug therapy problems.

OTHERWithout PHARMACEUTICAL CARE programe

Sponsors

TABREJ MUJAWAR
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
35 Years to No maximum
Healthy volunteers
No

Inclusion criteria

Inclusion Criteria: * Patients with type 2 diabetes mellitus of either * Patients with HbA1c more than 7% and * Patients with blood sugar level more than 140 mg / dl

Exclusion criteria

* Patient with end stage kidney disease. * Patient with heart failure. * Patient with chronic Diabetes problem and orthopedic problem

Design outcomes

Primary

MeasureTime frameDescription
Fasting blood glucose measurements recorded (mg/dl).Postprandial blood glucose Recorded: Fasting blood glucose measurements recorded (mg/dl).Postprandial bloodglucoseRecorded24 weeksFasting blood glucose measurements recorded (mg/dl).Postprandial blood glucose Recorded Fasting blood glucose measurements recorded (mg/dl).Postprandial blood glucose Recorded fasting blood glucose

Secondary

MeasureTime frameDescription
Quality of Life score24 weeksQuality of Life score

Countries

India

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026